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Structure of 914399-98-7
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)-2-methylpropanoic acid is a sterically hindered, bench-stable amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group and a tert-butoxy-substituted side chain. This configuration enhances solubility in organic solvents and improves coupling efficiency during solid-phase peptide synthesis. The chiral center at the alpha position ensures enantiomeric purity essential for sequence-specific assembly of biologically active peptides.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)-2-methylpropanoic acid serves as a robust, bench-stable chiral building block for peptide synthesis and heterocyclic scaffold construction. Its tert-butyl ester functionality enables selective deprotection under mild acidic conditions, while the Fmoc group ensures orthogonal protection during multi-step sequences. The sterically hindered α-methyl-α-alkoxy motif enhances diastereoselectivity in coupling reactions and facilitates purification via standard chromatographic methods.
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Lot numbers can be found on the outside label of a product: